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QA Specialist- GMP
Escape
West Lothian, West Lothian
Full-Time
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This is an exciting opportunity with an established and growing organisation specialising in the manufacture, supply and distribution of drug products. Based in West Lothian, they are looking for an experienced QA Specialist to join their team.
RESPONSIBILITIES INCLUDE
Managing vendor approval system (initial and review).
Maintaining vendor files electronically and physically.
Managing supplier performance and liaising with suppliers to complete investigations (vendor complaints) into supplier material defects.
Progress and manage vendor change notifications ensuring the correct departments have assessed the applicable changes.
Maintaining and updating vendor SOPs
Aid in the completion of technical agreements
To assist the Quality department in the overall implementation of the Quality function necessary for the maintenance of the quality management systems and related activities.
Provide general support to all Quality Unit activities relating to GMP, GCP, and other similar Quality Systems established within the company in order to ensure that the appropriate standards and effective working systems and relationships are maintained and where necessary improved throughout the company.
To identify and contribute to areas for improvement within the quality management systems to ensure compliant and efficient systems.
Provide input into the enhancement of quality policies, systems and procedures as appropriate.Candidate
Experience working in a QA role within a GMP environment
Strong follow-up skills and attention to detail
Ability to work independently
Competence in both written and verbal communication.
Ability to interact with personnel at all levels from a variety of disciplines
RESPONSIBILITIES INCLUDE
Managing vendor approval system (initial and review).
Maintaining vendor files electronically and physically.
Managing supplier performance and liaising with suppliers to complete investigations (vendor complaints) into supplier material defects.
Progress and manage vendor change notifications ensuring the correct departments have assessed the applicable changes.
Maintaining and updating vendor SOPs
Aid in the completion of technical agreements
To assist the Quality department in the overall implementation of the Quality function necessary for the maintenance of the quality management systems and related activities.
Provide general support to all Quality Unit activities relating to GMP, GCP, and other similar Quality Systems established within the company in order to ensure that the appropriate standards and effective working systems and relationships are maintained and where necessary improved throughout the company.
To identify and contribute to areas for improvement within the quality management systems to ensure compliant and efficient systems.
Provide input into the enhancement of quality policies, systems and procedures as appropriate.Candidate
Experience working in a QA role within a GMP environment
Strong follow-up skills and attention to detail
Ability to work independently
Competence in both written and verbal communication.
Ability to interact with personnel at all levels from a variety of disciplines
Recommended skills
Safety Assurance
Supplier Relationship Management
Good Clinical Practices (Gcp)
Attention To Detail
Good Manufacturing Practices
Quality Management Systems
Job ID: 212962352
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